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2-Fluoro-6-(4-Methylbenzyloxy)Benzonitrile

    • Product Name 2-Fluoro-6-(4-Methylbenzyloxy)Benzonitrile
    • Alias 2-Fluoro-6-[(4-methylphenyl)methoxy]benzonitrile
    • Einecs 812-645-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    741578

    Productname 2-Fluoro-6-(4-Methylbenzyloxy)Benzonitrile
    Casnumber 393515-14-1
    Molecularformula C15H12FNO
    Molecularweight 241.26 g/mol
    Appearance White to off-white solid
    Meltingpoint 71-75°C
    Purity ≥98%
    Solubility Soluble in organic solvents such as DMSO and dichloromethane
    Smiles Cc1ccc(cc1)COc2cccc(F)c2C#N
    Inchi InChI=1S/C15H12FNO/c1-11-4-6-13(7-5-11)8-18-15-9-3-2-12(16)14(15)10-17/h2-7,9H,8H2,1H3
    Storageconditions Store in a cool, dry place, protected from light

    As an accredited 2-Fluoro-6-(4-Methylbenzyloxy)Benzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass vial labeled "2-Fluoro-6-(4-Methylbenzyloxy)Benzonitrile, 1 gram," with tamper-evident cap and hazard symbols.
    Shipping 2-Fluoro-6-(4-Methylbenzyloxy)Benzonitrile is shipped in a tightly sealed container, protected from moisture and light. It is handled according to standard chemical transport regulations, with appropriate labeling for hazardous materials. Temperature and spill control measures are applied to ensure product integrity and safety during transit.
    Storage Store **2-Fluoro-6-(4-methylbenzyloxy)benzonitrile** in a cool, dry, well-ventilated area away from heat, ignition sources, and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from incompatible substances such as strong acids, bases, and oxidizers. Use only with appropriate chemical-resistant containers. Ensure access to a safety shower and eye wash station nearby.
    Application of 2-Fluoro-6-(4-Methylbenzyloxy)Benzonitrile

    Applications of 2-Fluoro-6-(4-Methylbenzyloxy)Benzonitrile in Industrial Manufacturing

    2-Fluoro-6-(4-Methylbenzyloxy)Benzonitrile serves as a key intermediate in advanced organic synthesis for several industrial segments. Its fluorinated aromatic structure and protected benzylic ether make it valuable in the scaling of fine chemicals, particularly where selective substitution and high purity are mandatory. Below are major application fields based on actual downstream demand and integration practices.

    1. Pharmaceutical Intermediate Synthesis for Oncology Drug APIs

    Many pharmaceutical companies utilize this compound in multi-step synthesis for targeted oncology APIs, including tyrosine kinase inhibitors. The fluorine and benzyloxy substituents support regioselective ring activation, critical for subsequent coupling or substitution. Manufacturers require precise control over residual solvents and byproducts, given the stringent batch release requirements for regulated active ingredients.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP General Chapter <232>: Elemental Impurities
    • EU GMP EudraLex Volume 4 (Part II)
    • Japanese Pharmacopoeia, Residue on Ignition, and Related Substances Monographs

    Typical usage ratio

    • Used at 0.8–1.2 molar equivalents relative to main coupling partner; adjusted based on reaction yield and conversion in pilot scale optimization

    Downstream process integration

    • Introduced after catalyst activation step, typically following palladium-catalyzed cross-coupling or nucleophilic substitution protocols in a closed reaction vessel under nitrogen

    Final product types

    • API intermediates for patent-protected oncology medications
    • Pilot lots of small-molecule kinase inhibitors
    • Reference standards for pharmaceutical QC
    • High purity benzamide derivatives for clinical research use

    2. Agricultural Chemical Intermediate for Fungicide Synthesis

    This compound plays a vital role as a coupling unit in the preparation of advanced fungicidal actives. Agrochemical companies integrate it to construct complex aromatic rings with electron-withdrawing features, crucial for the efficacy and environmental fate of the end product. Batch-to-batch consistency and compliance with environmental limits for aromatic byproducts are required for bulk sales in regulated markets.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals: Residues in Crops
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 for agrochemical manufacturing QC
    • EU Regulation 1107/2009 on Plant Protection Products

    Typical usage ratio

    • 0.9–1.5 molar equivalents per arylation or nucleophilic pathway, tailored to minimize unreacted residuals and comply with target purity levels (≥98%)

    Downstream process integration

    • Fed into the multi-stage synthesis platform after heterocycle formation, prior to oxidative deprotection and final formulation of technical-grade fungicide

    Final product types

    • Technical concentrate fungicides
    • Water-dispersible granular (WDG) crop protection formulations
    • Fungicidal active ingredient samples for efficacy trials
    • Analytical benchmarks for pesticide registration dossiers

    3. Advanced Material Intermediate for Liquid Crystal (LC) Compounds

    In the electronic materials sector, the compound acts as a fluorinated building block for manufacturing specialty liquid crystal substances used in high-performance LCDs. Manufacturers require strict contamination controls and enhanced purity profiles to prevent optical defects in finished display panels. Consistent lot analysis ensures that trace impurities do not impact downstream alignment or switching speed properties of LC blends.

    Industry compliance standards

    • IEC 60417 LCD and OLED Device Material Purity Guidelines
    • JEITA Standards for Organic Electronic Materials
    • ISO 14001:2015 Environmental Management in specialty chemical processing
    • RoHS Directive 2011/65/EU for hazardous substance restriction

    Typical usage ratio

    • 2–4% by weight in masterbatch formulations for LC precursor synthesis, precise ratio adjusted for desired dielectric and birefringence outcomes

    Downstream process integration

    • Added during the pre-polymer blending step in LC monomer production, followed by controlled polymerization and refinement under high vacuum

    Final product types

    • Liquid crystal display (LCD) materials for TVs and monitors
    • Smartphone and tablet display panel substances
    • Performance-tuned LC formulations for automotive and medical screens
    • Quality control standards for electronic material suppliers

    4. Specialty Chemical for Photoinitiator Synthesis

    Manufacturers of UV-curable coatings and inks employ this benzonitrile derivative as a precursor in the synthesis of customized photoinitiators. Its structure allows precise functionalization to control light absorption and radical initiation rates, a critical factor for industrial inkjet and 3D printing processes. Stringent oversight ensures compliance with residual monomer and migration limits in end-use packaging.

    Industry compliance standards

    • REACH regulation (EC) No 1907/2006, SVHC monitoring
    • Swiss Ordinance on Packaging Inks (SR 817.023.21) migration limits
    • ASTM D7767 Standard for UV-Curable Ink Raw Material Purity
    • ISO 22000:2018, if integrated into food packaging printing

    Typical usage ratio

    • 3–7% by weight in photoinitiator core compound synthesis, finalized based on reactivity and light intensity testing in target curing systems

    Downstream process integration

    • Introduced during the cyclization or quaternization stages of photoinitiator molecule assembly, prior to final purification and blending with UV-curable resins

    Final product types

    • UV-curable photoinitiator concentrates
    • Specialty inkjet printing fluids
    • 3D printing resin chemistry
    • Migration-tested UV ink formulations for direct food contact

    5. Intermediate in Fluorinated Aromatic Polymers for High-Performance Coatings

    Producers of performance coatings utilize the compound as a monomeric precursor for creating fluorinated aromatic polymers with enhanced chemical resistance and surface properties. The methylbenzyloxy protection allows for controlled de-protection steps, critical for achieving desired polymer architecture and stability. Strict raw material monitoring and traceability ensure uniformity in high-value coating lots.

    Industry compliance standards

    • ISO 12944-6:2018 Paints and varnishes—Performance standards for industrial protective coatings
    • ASTM D4752: Standard Test Method for Measuring MEK Resistance of Film
    • GHS for chemical labeling and safety in manufacture
    • EPA TSCA Inventory Listing (if supplied for US market)

    Typical usage ratio

    • 1–10% mole fraction in copolymerizations, with adjustments based on desired surface energy and chemical resistance for coatings on metals or electronics

    Downstream process integration

    • Fed into controlled polymerization reactors following catalyst charging and solvent calibration; methylbenzyloxy group allows for strategic side-chain modifications before curing

    Final product types

    • High-end anti-corrosion coatings for aerospace and marine application
    • Protective films for electronic circuitry
    • Solvent-resistant paints for industrial tool surfaces
    • Polymer standards for coating performance benchmarking
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